4.7 Article

Functional Mapping of the Zebrafish Early Embryo Proteome and Transcriptome

期刊

JOURNAL OF PROTEOME RESEARCH
卷 13, 期 12, 页码 5536-5550

出版社

AMER CHEMICAL SOC
DOI: 10.1021/pr5005136

关键词

Zebrafish; proteomics; transcriptomics; early embryo; development; functional mapping

资金

  1. Agency for Science, Technology and Research (A*STAR), Singapore

向作者/读者索取更多资源

Zebrafish is a popular system for studying vertebrate development and disease that shows high genetic conservation with humans. Molecular level studies at different stages of development are essential for understanding the processes deployed during ontogeny. Here, we performed comparative analysis of the whole proteome and transcriptome of the early stage (24 h post-fertilization) zebrafish embryo. We identified 8363 proteins with their approximate cellular abundances (the largest number of zebrafish embryo proteins quantified thus far), through a combination of thorough deyolking and extensive fractionation procedures, before resolving the peptides by mass spectrometry. We performed deep sequencing of the transcripts and found that the expressed proteome and transcriptome displayed a moderate correlation for the majority of cellular processes. Integrative functional mapping of the quantified genes demonstrated that embryonic developmental systems differentially exploit transcriptional and post-transcriptional regulatory mechanisms to modulate protein abundance. Using network mapping of the low-abundance proteins, we identified various signal transduction pathways important in embryonic development and also revealed genes that may be regulated at the post-transcriptional level. Our data set represents a deep coverage of the functional proteome and transcriptome of the developing zebrafish, and our findings unveil molecular regulatory mechanisms that underlie embryonic development.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Biochemistry & Molecular Biology

Dolastatin 15 from a Marine Cyanobacterium Suppresses HIF-1α Mediated Cancer Cell Viability and Vascularization

Ranjala Ratnayake, Sarath P. Gunasekera, Jia Jia Ma, Long H. Dang, Thomas J. Carney, Valerie J. Paul, Hendrik Luesch

CHEMBIOCHEM (2020)

Letter Dermatology

Huriez syndrome caused by a large deletion that abrogates the skin-specific isoform of SMARCAD1

A. Y. T. Loh, C. M. Ho, S. Muthiah, B. Venkatesh, S. Zwolinski, A. P. J. J. Bray, B. Reversade, N. Rajan, T. J. Carney

BRITISH JOURNAL OF DERMATOLOGY (2021)

Article Multidisciplinary Sciences

Proximity proteomics identifies PAK4 as a component of Afadin-Nectin junctions

Yohendran Baskaran, Felicia Pei-Ling Tay, Elsa Yuen Wai Ng, Claire Lee Foon Swa, Sheena Wee, Jayantha Gunaratne, Edward Manser

Summary: The study reveals the association of PAK4 with Afadin-dependent cell-cell junctions and identifies potential phosphorylation substrates of PAK4. Within the cellular environment, PAK4 is found to be linked to Afadin and the nectin family of junctional proteins; PAK4 depends on Afadin for its localization at cell-cell junctions.

NATURE COMMUNICATIONS (2021)

Article Biology

Matriptase activation of Gq drives epithelial disruption and inflammation via RSK and DUOX

Jiajia Ma, Claire A. Scott, Ying Na Ho, Harsha Mahabaleshwar, Katherine S. Marsay, Changqing Zhang, Christopher Kj Teow, Ser Sue Ng, Weibin Zhang, Vinay Tergaonkar, Lynda J. Partridge, Sudipto Roy, Enrique Amaya, Tom J. Carney

Summary: This study reveals that mutations in the hai1a gene in zebrafish lead to a series of cellular responses, including inflammation and calcium signaling, without inducing epithelial cell motility. Inhibition of the Gq subunit can rescue these abnormal phenotypes, and increased MAPK pathway activity may be the cause of epidermal defects.
Article Biochemical Research Methods

Label-free quantitative measurement of cardiovascular dynamics in a zebrafish embryo using frequency-comb-referenced-quantitative phase imaging

Jeeranan Boonruangkan, Hamid Farrokhi, Thazhe M. Rohith, Samuel Kwok, Tom J. Carney, Pei-Chen Su, Young-Jin Kim

Summary: This study successfully measured heart rate and blood flow in zebrafish embryos using FCR-QPI technique, revealing the average velocity of RBCs and heart rate at different stages of development.

JOURNAL OF BIOMEDICAL OPTICS (2021)

Article Multidisciplinary Sciences

Tetraspanin Cd9b and Cxcl12a/Cxcr4b have a synergistic effect on the control of collective cell migration

Katherine S. Marsay, Sarah Greaves, Harsha Mahabaleshwar, Charmaine Min Ho, Henry Roehl, Peter N. Monk, Tom J. Carney, Lynda J. Partridge

Summary: Collective cell migration of the posterior lateral line primordium in zebrafish development is modulated by Cd9, which contributes to effective chemokine signaling. Cd9a and Cd9b function partially redundantly in pLLP migration, with their loss leading to delayed migration and reduced neuromast numbers. Loss of both Cd9a and Cd9b sensitizes embryos to reduced levels of Cxcr4b and Cxcl12a.

PLOS ONE (2021)

Article Cell Biology

Transcriptome Profiling of Osteoblasts in a Medaka (Oryzias latipes) Osteoporosis Model Identifies Mmp13b as Crucial for Osteoclast Activation

Ranran Liu, Nurgul Imangali, Lalith Prabha Ethiraj, Tom James Carney, Christoph Winkler

Summary: In this study, transcriptome profiling of bone cells in a medaka model was used to identify the crucial role of mmp13b gene in bone remodeling and homeostasis. Mmp13b mutants exhibited impaired osteoclast activity and inability to degrade unmineralized collagens and mineralized bone matrix. The lack of mmp13b also resulted in immature and non-activated osteoclasts and delayed fin regeneration.

FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2022)

Article Genetics & Heredity

Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome

Abigail Y. T. Loh, Sanja Spoljar, Granville Y. W. Neo, Nathalie Escande-Beillard, Marc Leushacke, Monique N. H. Luijten, Byrappa Venkatesh, Carine Bonnard, Maurice A. M. van Steensel, Henning Hamm, Andrew Carmichael, Neil Rajan, Thomas J. Carney, Bruno Reversade

Summary: Huriez syndrome is a rare genetic skin disorder characterized by scleroatrophic hands and feet, hypoplastic nails, palmoplantar keratoderma, and a predisposition to cutaneous squamous cell carcinoma. This study reported three HRZ families from different regions and identified germline SMARCAD1 pathogenic variants. The findings suggest that Huriez syndrome may be allelic to Adermatoglyphia and Basan syndrome, sharing similar genetic and phenotypic features.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2022)

Article Fisheries

Robust non-toxic macroscale beads with antibacterial and contaminant scavenging properties for aquaculture

Penghui Zhang, Tom J. Carney, Karin Schroen, Remko M. Boom, Mary B. Chan-Park

Summary: Crosslinked beads prepared by diffusion-driven layer by layer process exhibit excellent antibacterial activity and biocompatibility, with high adsorption capacity for removing fish waste.

AQUACULTURE (2022)

Article Cell Biology

Colorimetric and fluorescent TRAP assays for visualising and quantifying fish osteoclast activity

Lalith Prabha Ethiraj, En Lei Samuel Fong, Ranran Liu, Madelynn Chan, Christoph Winkler, Tom James Carney

Summary: In this study, we developed simple colorimetric and fluorescent TRAP assays in zebrafish and medaka, which can be used to assess osteoclast activity. Fluorescent TRAP staining using the ELF97 substrate is a rapid, stable system that is compatible with other fluorescence stains, transgenic lines, and antibody approaches.

EUROPEAN JOURNAL OF HISTOCHEMISTRY (2022)

Article Biochemistry & Molecular Biology

Slit-Robo signalling establishes a Sphingosine-1-phosphate gradient to polarise fin mesenchyme

Harsha Mahabaleshwar, P. Asharani, Tricia Yi Loo, Shze Yung Koh, Melissa R. Pitman, Samuel Kwok, Jiajia Ma, Bo Hu, Fang Lin, Xue Li Lok, Stuart M. Pitson, Timothy E. Saunders, Tom J. Carney

Summary: Mesenchymal cell immigration into growing fins and limb buds drives distal outgrowth, with tensile forces between these cells essential for fin and limb morphogenesis. Morphogens derived from the apical fin domain regulate cell polarity, migration, division, and adhesion of limb mesenchyme cells. The mutant stomp in zebrafish displays defects in fin morphogenesis, including blister formation and loss of orientation and adhesion of immigrating fin mesenchyme cells. The gene encoding Slit3, an axon guidance ligand, is found to be mutated in stomp. Slit ligands derived from immigrating mesenchyme act via Robo receptors at the apical ectodermal ridge (AER) to promote the release of sphingosine-1-phosphate (S1P), which then diffuses back to the mesenchyme to regulate their polarization, orientation, positioning, and adhesion to the interstitial matrix of the fin fold.

EMBO REPORTS (2022)

Article Cell Biology

Aerobic glycolysis is important for zebrafish larval wound closure and tail regeneration

Claire A. Scott, Tom J. Carney, Enrique Amaya

Summary: The mechanisms of appendage regeneration are still largely unknown, and metabolic reprogramming plays an important role in the process. This study used a genetically encoded biosensor called Laconic to evaluate lactate levels during fin regeneration in zebrafish. The findings showed a rapid increase in lactate levels following injury, with a role of aerobic glycolysis in actomyosin contraction and wound closure. Additionally, a second wave of lactate production was observed during larval tail regeneration. Inhibiting glycolysis hindered wound contraction and tissue regrowth, indicating the necessity of aerobic glycolysis at two distinct stages of regeneration.

WOUND REPAIR AND REGENERATION (2022)

Article Multidisciplinary Sciences

Hypoxia deactivates epigenetic feedbacks via enzyme-derived clicking proteolysis-targeting chimeras

Thang Cong Do, Jun Wei Lau, Caixia Sun, Songhan Liu, Khoa Tuan Kha, Seok Ting Lim, Yu Yang Oon, Yuet Ping Kwan, Jia Jia Ma, Yuguang Mu, Xiaogang Liu, Thomas James Carney, Xiaomeng Wang, Bengang Xing

Summary: ENCTACs, by specifically degrading BET protein BRD4 and modulating hypoxic signaling, provide a precise treatment approach for cancer.

SCIENCE ADVANCES (2022)

Article Multidisciplinary Sciences

Zebrafish pigment cells develop directly from persistent highly multipotent progenitors

Tatiana Subkhankulova, Karen Camargo Sosa, Leonid A. Uroshlev, Masataka Nikaido, Noah Shriever, Artem S. Kasianov, Xueyan Yang, Frederico S. L. M. Rodrigues, Thomas J. Carney, Gemma Bavister, Hartmut Schwetlick, Jonathan H. P. Dawes, Andrea Rocco, Vsevolod J. Makeev, Robert N. Kelsh

Summary: Neural crest cells are highly multipotent stem cells, and it is still unclear how their fate restriction to specific fates occurs. This study shows that in zebrafish, broad multipotency is retained even after migration, suggesting that fate restriction occurs directly but dynamically.

NATURE COMMUNICATIONS (2023)

暂无数据